Pérez-Acevedo Ana Pilar, Busardò Francesco Paolo, Pacifici Roberta, Mannocchi Giulio, Gottardi Massimo, Poyatos Lourdes, Papaseit Esther, Pérez-Mañá Clara, Martin Soraya, Di Trana Annagiulia, Pichini Simona, Farré Magí
Clinical Pharmacology Unit, Hospital Universitari Germans Trias i Pujol and Institut de Recerca Germans Trias i Pujol (HUGTiP-IGTP), 08916 Badalona, Spain.
Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Cerdanyola del Vallés, 08193 Bellaterra, Spain.
Pharmaceuticals (Basel). 2020 Dec 12;13(12):459. doi: 10.3390/ph13120459.
The use of cannabis flowering tops with standardized amounts of active phytocannabinoids was recently authorized in several countries to treat several painful pathological conditions. The acute pharmacological effects and disposition of Δ-9-tetrahydrocannabinol (THC), cannabidiol (CBD), their acidic precursors and THC metabolites after oil and decoction administration have been already described. In this study, the disposition of CBD metabolites: 7-carboxy-cannabidiol (7-COOH-CBD), 7-hydroxycannabidiol (7-OH-CBD), 6-α-hydroxycannabidiol (6-α-OH-CBD), and 6-β-hydroxycannabidiol (6-β-OH-CBD) in the serum and urine of healthy volunteers was presented. Thirteen healthy volunteers were administered 100 mL of cannabis decoction in the first experimental session and, after 15 days of washout, 0.45 mL of oil. Serum and urine samples were collected at different time points, and the CBD metabolites were quantified by ultra-high-performance liquid chromatography-tandem mass spectrometry. The most abundant serum metabolite was 7-COOH-CBD, followed by 7-OH-CBD, 6-β-OH-CBD, and6-α-OH-CBD, after decoction and oil. Both 7-OH-CBD and the 6-α-OH-CBD showed similar pharmacokinetic properties following administration of both cannabis preparations, whereas 7-COOH and 6-α-OH-CBD displayed a significant higher bioavailability after decoction consumption. All CBD metabolites were similarly excreted after oil and decoction intake apart from 6-α-OH-CBD, which had a significantly lower excretion after oil administration. The pharmacokinetic characterization of CBD metabolites is crucial for clinical practice since the cannabis herbal preparations are increasingly used for several pathological conditions.
最近,一些国家已批准使用含有标准化活性植物大麻素量的大麻花顶来治疗多种疼痛性病理状况。此前已经描述了油剂和煎剂给药后Δ-9-四氢大麻酚(THC)、大麻二酚(CBD)、它们的酸性前体以及THC代谢物的急性药理作用和处置情况。在本研究中,展示了健康志愿者血清和尿液中大麻二酚代谢物:7-羧基-大麻二酚(7-COOH-CBD)、7-羟基大麻二酚(7-OH-CBD)、6-α-羟基大麻二酚(6-α-OH-CBD)和6-β-羟基大麻二酚(6-β-OH-CBD)的处置情况。在第一个实验环节,13名健康志愿者服用了100毫升大麻煎剂,在洗脱15天后,服用了0.45毫升油剂。在不同时间点采集血清和尿液样本,并通过超高效液相色谱-串联质谱法定量分析大麻二酚代谢物。服用煎剂和油剂后,血清中最丰富的代谢物是7-COOH-CBD,其次是7-OH-CBD、6-β-OH-CBD和6-α-OH-CBD。服用两种大麻制剂后,7-OH-CBD和6-α-OH-CBD均表现出相似的药代动力学特性,而服用煎剂后,7-COOH和6-α-OH-CBD的生物利用度显著更高。除6-α-OH-CBD外,服用油剂和煎剂后,所有大麻二酚代谢物的排泄情况相似,6-α-OH-CBD在服用油剂后的排泄量显著更低。大麻二酚代谢物的药代动力学特征对临床实践至关重要,因为大麻草药制剂越来越多地用于多种病理状况。